FDA 510(k) Applications Submitted by DOUGLAS FULTON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K160222	01/29/2016	OIC Cervical PEEK Spacer	THE ORTHOPAEDIC IMPLANT COMPANY
K140357	02/12/2014	OIC VARIABLE ANGLE SMALL FRAGMENT LOCKING PLATE SYSTEM	ORTHOPAEDIC IMPLANT COMPANY
K150655	03/13/2015	OIC Intramedullary Nail System	ORTHOPAEDIC IMPLANT COMPANY
K211112	04/14/2021	OIC External Fixation System	Orthopaedic Implant Company
K171211	04/25/2017	OIC External Fixation System	Orthopaedic Implant Company
K181184	05/03/2018	OIC Intramedullary Nail System	The Orthopaedic Implant Company
K212601	08/17/2021	DRPx Locking Distal Radius Plate System	Orthopaedic Implant Company
K242995	09/26/2024	OIC Small / Mini Fragment Plate System	The Orthopaedic Implant Company
K182736	09/28/2018	OIC Suture Anchor System	The Orthopaedic Implant Company
K202971	09/30/2020	DRPx Locking Distal Radius Plate System	Orthopaedic Implant Company
K223118	10/03/2022	OIC Variable Angle Small Fragment Locking Plate System	Orthopaedic Implant Company
K233531	11/02/2023	OIC FLEX-FIXÖ System	Orthopaedic Implant Company
K223761	12/15/2022	OIC Intramedullary Screw System	Orthopaedic Implant Company
K183682	12/28/2018	OIC External Fixation System	Orthopaedic Implant Company